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Pyridine
[CAS# 110-86-1]

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Complete supplier list of Pyridine
Identification
Classification Flavors and spices >> Synthetic spice >> Lactone and oxygen-containing heterocyclic compound >> Thiazole, thiophene and pyridine
Name Pyridine
Synonyms Azabenzene
Molecular Structure CAS # 110-86-1, Pyridine, Azabenzene
Molecular Formula C5H5N
Molecular Weight 79.10
CAS Registry Number 110-86-1
EC Number 203-809-9
FEMA 2966
SMILES C1=CC=NC=C1
Properties
Density 0.978
Melting point -42 ºC
Boiling point 115-116 ºC
Refractive index 1.5085-1.5105
Flash point 17 ºC
Water solubility Miscible
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS07 Danger    Details
Hazard Statements H225-H302-H312-H315-H319-H332    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P317-P321-P330-P332+P317-P337+P317-P362+P364-P370+P378-P403+P235-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H332
Flammable liquidsFlam. Liq.2H225
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H312
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Skin sensitizationSkin Sens.1BH317
Serious eye damageEye Dam.1H318
Eye irritationEye Irrit.2H320
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.3H301
Eye irritationEye Irrit.2AH319
Skin corrosionSkin Corr.1CH314
Specific target organ toxicity - repeated exposureSTOT RE1H372
Specific target organ toxicity - single exposureSTOT SE3H336
ExplosivesExpl.1.1H201
Acute toxicityAcute Tox.2H330
Specific target organ toxicity - repeated exposureSTOT RE2H373
Acute toxicityAcute Tox.3H312
CarcinogenicityCarc.2H351
Specific target organ toxicity - single exposureSTOT SE1H370
Acute hazardous to the aquatic environmentAquatic Acute1H400
Reproductive toxicityRepr.2H361
Transport Information UN 1282
SDS Available
up Discovory and Applicatios
Pyridine is a heterocyclic organic compound characterized by its six-membered aromatic ring containing one nitrogen atom. With the molecular formula C5H5N, pyridine is a colorless liquid with a distinct, unpleasant odor resembling that of rotten fish. It is highly soluble in water and polar solvents, making it a versatile solvent and reagent in various chemical reactions. The discovery of pyridine dates back to 1849, when the German chemist August Wilhelm von Hofmann first isolated it from coal tar during his research into the products of coal combustion.

Hofmann’s discovery was pivotal, as it not only introduced pyridine to the scientific community but also opened avenues for its application in organic chemistry and industrial processes. The compound was subsequently synthesized in the laboratory, and various derivatives were developed, expanding its utility across multiple fields. Pyridine's unique structure and chemical properties make it a key intermediate in the synthesis of numerous organic compounds.

One of the primary applications of pyridine is as a precursor to the production of agrochemicals, including herbicides, insecticides, and fungicides. Pyridine derivatives play a significant role in the synthesis of important agricultural chemicals, enhancing crop protection and pest management. Compounds such as picloram, a herbicide derived from pyridine, have been extensively used in agricultural practices for their effectiveness in controlling unwanted plant species.

In addition to agriculture, pyridine is widely utilized in the pharmaceutical industry. It serves as a building block for the synthesis of various pharmaceutical compounds, including analgesics, anti-inflammatory agents, and antiviral drugs. The ability to modify the pyridine ring through substitution reactions allows chemists to create a diverse range of active pharmaceutical ingredients. Pyridine-based compounds such as isoniazid and nicotinic acid have been instrumental in treating diseases like tuberculosis and improving overall health.

Pyridine is also employed as a solvent and reagent in organic synthesis. Its polar nature and ability to form coordination complexes with metal ions make it an effective solvent for various chemical reactions. Pyridine is used in the synthesis of dyes, resins, and other fine chemicals, contributing to the development of diverse products in the chemical industry. Furthermore, it serves as a catalyst in reactions such as the synthesis of heterocyclic compounds and as a medium for electrophilic substitutions.

While pyridine has valuable applications, it is essential to consider its toxicity and potential health effects. Exposure to pyridine can lead to irritation of the skin, eyes, and respiratory system. As such, proper safety measures and protocols are critical when handling this compound in industrial and laboratory settings. Regulatory agencies have established guidelines to ensure the safe use of pyridine and its derivatives, balancing the benefits of its applications with potential risks.

In conclusion, pyridine is a significant organic compound with a rich history dating back to the 19th century. Its diverse applications span agriculture, pharmaceuticals, and organic synthesis, making it a valuable resource in various industries. As research continues to explore new derivatives and applications, pyridine is poised to maintain its importance in the field of organic chemistry.
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